The Minor "A" allele is associated with:

  • Increased risk of Crohn's disease [R].

This SNP is associated with (unknown alleles):

  • associated with levels of vitamin B(12) in Indian population  [R]

rs602662

Parent Gene: FUT2

Importance: 3
Less common allele: A = 33%
More common allele: G = 67%
My Genotype: Log In
Risk Allele: A, G, A

Disease/Trait: Vitamin B12 Measurement

The A allele of rs602662 is reported to be associated with Vitamin B12 Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Vitamin B12 levels.

Disease/Trait: Systemic Lupus Erythematosus

The G allele of rs602662 is reported to be associated with Systemic Lupus Erythematosus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Autoimmune Disease

The G allele of rs602662 is reported to be associated with Autoimmune Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Crohn's Disease

The G allele of rs602662 is reported to be associated with Crohn's Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Ulcerative Colitis

The G allele of rs602662 is reported to be associated with Ulcerative Colitis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Celiac Disease

The G allele of rs602662 is reported to be associated with Celiac Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Psoriasis

The G allele of rs602662 is reported to be associated with Psoriasis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Ankylosing Spondylitis

The G allele of rs602662 is reported to be associated with Ankylosing Spondylitis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Chronic Childhood Arthritis

The G allele of rs602662 is reported to be associated with Chronic Childhood Arthritis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Common Variable Immunodeficiency

The G allele of rs602662 is reported to be associated with Common Variable Immunodeficiency (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Type I Diabetes Mellitus

The G allele of rs602662 is reported to be associated with Type I Diabetes Mellitus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Autoimmune Thyroid Disease

The G allele of rs602662 is reported to be associated with Autoimmune Thyroid Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Vitamin B12 Measurement

rs602662 is associated with Vitamin B12 Measurement (R) . It is reported to have a 0.07 unit decrease on Folate pathway vitamin levels (Plasma Vitamin B12). No specific risk allele was identified in the study.

Disease/Trait: Vitamin B12 Measurement

The A allele of rs602662 is reported to be associated with Vitamin B12 Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Folate pathway vitamin levels (vitamin B12).